EP0951337B1 - Process for recovering cf 4? and c 2?f 6? from a gas - Google Patents
Process for recovering cf 4? and c 2?f 6? from a gas Download PDFInfo
- Publication number
- EP0951337B1 EP0951337B1 EP97952294A EP97952294A EP0951337B1 EP 0951337 B1 EP0951337 B1 EP 0951337B1 EP 97952294 A EP97952294 A EP 97952294A EP 97952294 A EP97952294 A EP 97952294A EP 0951337 B1 EP0951337 B1 EP 0951337B1
- Authority
- EP
- European Patent Office
- Prior art keywords
- process according
- stream
- vent gas
- gas
- membrane
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
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Classifications
-
- C—CHEMISTRY; METALLURGY
- C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
- C25C—PROCESSES FOR THE ELECTROLYTIC PRODUCTION, RECOVERY OR REFINING OF METALS; APPARATUS THEREFOR
- C25C3/00—Electrolytic production, recovery or refining of metals by electrolysis of melts
- C25C3/06—Electrolytic production, recovery or refining of metals by electrolysis of melts of aluminium
- C25C3/22—Collecting emitted gases
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D53/00—Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols
- B01D53/22—Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols by diffusion
- B01D53/229—Integrated processes (Diffusion and at least one other process, e.g. adsorption, absorption)
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D2257/00—Components to be removed
- B01D2257/20—Halogens or halogen compounds
Definitions
- the present invention generally relates to a gas separation process.
- the invention particularly relates to a process for removing at least one of CF 4 and C 2 F 6 from a gas stream using a membrane.
- the invention also particularly relates to a method of making aluminum, which method includes removing at least one of CF 4 and C 2 F 6 from a gas stream using a membrane.
- the first step involves extracting alumina (Al 2 O 3 ) from bauxite using a Bayer process.
- the second step involves reducing the alumina which is dissolved in a mixture of molten cryolite (Na 3 AlF 6 ) and aluminum trifluoride (AlF 3 ) in an electrolysis cell at about 950 to 960 C using the Hall-Heroult process.
- AlF 3 aluminum trifluoride
- aluminum-containing ions are reduced electrochemically to produce metallic aluminum at the metal cathode surface.
- the electrolysis cell approaches an anode effect. This approach is characterized by the following events:
- the emission rate of CF 4 and C 2 F 6 per day is 0.25 kg. There are normally 100 to 200 cells per plant. Therefore, the daily emission of CF 4 and C 2 F 6 per plant is about 50 kg.
- the present invention relates to a process for recovering at least one of CF 4 and C 2 F 6 from a vent gas from an aluminum electrolysis cell.
- the process comprises the steps of:
- the present invention relates to a method of making aluminum.
- the method includes the steps of:
- the present invention relates to a process for removing at least one of CF 4 and C 2 F 6 from a gas stream.
- the present invention relates to a process for removing both CF 4 and C 2 F 6 from a gas stream containing the same.
- the gas stream Prior to separation, the gas stream preferably contains from about 0.01 to about 20% by volume of at least one of CF 4 and C 2 F 6 .
- the gas stream can include oxygen, carbon dioxide, and nitrogen as well as other gaseous components.
- the process according to the present invention comprises the step of contacting the gas stream with a membrane at conditions effective to obtain a retentate stream rich in at least one of CF 4 and C 2 F 6 , and a permeate stream depleted in at least one of CF 4 and C 2 F 6 .
- the retentate stream is depleted in oxygen, carbon dioxide, and nitrogen while the permeate stream is rich in oxygen, carbon dioxide, and nitrogen.
- the contacting step preferably produces a retentate stream rich in both CF 4 and C 2 F 6 , and a permeate stream depleted in both CF 4 and C 2 F 6 .
- the term “rich” means that the concentration of a particular component in that stream is greater than the concentration of the same component in the feed stream.
- the term “depleted” means that the concentration of a particular component in that stream is less than the concentration of the same component in the feed stream.
- the retentate stream preferably comprises from about 25 to about 100% by volume of at least one of CF 4 and C 2 F 6 .
- the permeate stream preferably comprises from about 0 to about 0.01% by volume of at least one of CF 4 and C 2 F 6 .
- the purity of the permeate and retentate streams is improved by contacting the streams with additional membranes arranged in series.
- Such a process may be carried out according to the multi-step membrane separation system shown in Figure 3.
- each of the permeate and retentate streams may be passed to another membrane contacting unit to increase the purity of the stream.
- the number of contacting steps "m" and "n” may vary depending on the purity desired.
- Any membrane can be used in the process according to the present invention so long as the membrane can selectively retain at least one of CF 4 and C 2 F 6 while passing the other components in the gas stream through.
- the membrane should also be substantially non-reactive with the gaseous components to be separated.
- Membranes useful in the invention are preferably glassy membranes such as polymer membranes made preferably from polyimides; polyamides; polyamide-imides; polyesters polycarbonates; polysulfones; polyethersulfone; polyetherketone; alkyl substituted aromatic polyesters; blends of polyethersulfone, aromatic polyimides, aromatic polyamides, polyamides-imides, fluorinated aromatic polyimide, polyamide, and polyamide-imides; glassy polymeric membranes such as those disclosed US 5,599,380; cellulose acetates; and blends thereof, copolymers thereof, substituted polymers (e.g. alkyl, aryl) thereof and the like.
- glassy membranes such as polymer membranes made preferably from polyimides; polyamides; polyamide-imides; polyesters polycarbonates; polysulfones; polyethersulfone; polyetherketone; alkyl substituted aromatic polyesters; blends of polyethersulfone, aromatic polyimides,
- Asymmetric membranes are prepared by the precipitation of polymer solutions in solvent-miscible nonsolvents. Such membranes are typified by a dense separating layer supported on an anisotropic substrate of a graded porosity and are generally prepared in one step. Examples of such membranes and their methods of manufacture are disclosed in U.S. Patent Nos. 4,113,628; 4,378,324; 4,460,526; 4,474,662; 4,485,056; 4,512,893; 5,085,676; and 4,717,394 .
- the '394 and '676 patents disclose preparation of asymmetric separation membranes from selected polyimides. Particularly preferred membranes are polyimide asymmetric gas separation membranes as disclosed in the '676 patent.
- one side of the gas separation membrane is contacted with a complex multicomponent gas mixture and certain of the gases of the mixture permeate through the membrane faster than the other gases.
- Gas separation membranes thereby allow some gases to permeate through them while serving as a barrier to other gases in a relative sense.
- the relative gas permeation rate through the membrane is a property of the membrane material composition and its morphology. It has been suggested in the prior art that the intrinsic permeability of a polymer membrane is a combination of gas diffusion through the membrane, controlled in part by the packing and molecular free volume of the material, and gas solubility within the material. Selectivity is the ratio of the permeabilities of two gases being separated by a material. It is also highly desirable to form defect-free dense separating layers in order to retain high gas selectivity.
- Composite gas separation membranes typically have a dense separating layer on a preformed microporous substrate.
- the separating layer and the substrate are usually different in composition.
- Composite gas separation membranes have evolved to a structure of an ultrathin, dense separating layer supported on an anisotropic, microporous substrate. These composite membrane structures can be prepared by laminating a preformed ultrathin dense separating layer on top of a preformed anisotropic support membrane. Examples of such membranes and their methods of manufacture are disclosed in U.S. Patent Nos.
- composite gas separation membranes may be prepared by multistep fabrication processes, wherein first an anisotropic, porous substrate is formed, followed by contacting the substrate with a membrane-forming solution. Examples of such methods are described in U.S. Patent Nos. 4,826,599; 3,648,845; and 3,508,994.
- the membrane can be post-treated with, or coated by, or co-extruded with, a fluorinated or perfluorinated polymer layer in order to increase its ability to withstand harmful constituents in the gas mixture from which PFCs are to be separate, at low levels or temporary contact with such components.
- the hollow-fiber spinning process depends on many variables which may affect the morphology and properties of the hollow-fiber membrane. These variables include the composition of the polymer solution employed to form the fiber, the composition of fluid injected into the bore of the hollow-fiber extrudate during spinning, the temperature of the spinneret, the coagulation medium employed to treat the hollow-fiber extrudate, the temperature of the coagulation medium, the rapidity of coagulation of the polymer, the rate of extrusion of the fiber, takeup speed of the fiber onto the takeup roll, and the like.
- the temperature of the gas mixture and/or the membrane during the contacting step can vary from about -10°C to about 100°C.
- the temperature is between about 10°C and 80°C. More preferably, the temperature ranges from ambient, i.e., from about 20°C to 25°C, to about 60°C.
- a pressure drop across the membrane of less than about 1.4 x 10 7 Pa (2,000 psig). More preferably, the pressure drop ranges from about 2 x 10 4 Pa (3 psig) to about 1.4 x 10 6 Pa (200 psig). Even more preferably, the pressure drop is about 1.4 x 10 5 Pa (20 psig) to about 4.1 x 10 5 Pa (60 psig).
- the requisite pressure drop across the membrane can be provided in one of two ways.
- the feed gas stream can be compressed.
- Preferred compressors are sealed and oil-free, such as the compressors sold under the tradename POWEREX, available from the Powerex Harrison Company of Ohio.
- the pressure drop across the membrane can be established by lowering the pressure on the permeate side of the membrane. To create the lower pressure on the permeate side, a vacuum pump or any other suction device can be used.
- the flowrate of the gas stream across the membrane can vary from about 0 to about 10 5 Nm 3 /h per square meter of membrane available for separation.
- the flowrate is from about 10 -4 to about 10 Nm 3 /h-m 2 . More preferably, the flowrate is from about 0.1 to about 0.5 Nm 3 /h-m 2 .
- the present invention relates to a process for recovering at least one of CF 4 and C 2 F 6 from a vent gas from an aluminum electrolysis cell.
- the vent gas comprises (1) gaseous components such as O 2 , CO 2 , and N 2 ; (2) inorganic fluorides such as F 2 , HF, and NaAlF 4 ; and (3) at least one of CF 4 and C 2 F 6 .
- the vent gas can also include some hydrocarbons and a large amount of particulates.
- the first step in this process involves removing the inorganic fluorides from the vent gas to produce a purified vent gas.
- the inorganic fluorides are preferably removed from the vent gas by using a caustic scrubber.
- the scrubber can be wet or dry. Dry scrubbers are usually resin-type scrubbers or soda-lime, while some dry scrubbers comprising catalysts such as MnO 2 can also be used. Exemplary wet scrubbers that can be used in the present invention are described in the brochure entitled, "Selecting a CDOTM for Your Particular Application" from DELATECH Corporation, which brochure is hereby incorporated by reference. When various harmful constituents have to be removed, it is preferred to use a dry scrubber or scrubbers in series with a wet scrubber or scrubbers.
- one or more filters are employed to remove the particulates from the vent gas. It is preferred to use a filter having a pore size diameter of less than 20 micrometers, and more preferably, less than 10 micrometers.
- the second step in this process involves contacting the purified vent gas with a membrane at conditions effective to obtain a retentate stream rich in at least one of CF 4 and C 2 F 6 , and a permeate stream depleted in at least one of CF 4 and C 2 F 6 .
- This membrane separation step can be carried out as described above.
- the present invention relates to a method of making aluminum.
- the method includes the steps of:
- Figure 1 The general features of this method are illustrated in Figure 1. Referring to Figure 1, a stream 1 of alumina, cryolite, and aluminum trifluoride is fed into an aluminum electrolyzing cell 2 where molten aluminum is produced by electrolytically reducing the alumina. The operating conditions and equipment necessary to carry out this step are well known to those skilled in the art.
- the molten aluminum is then withdrawn from the electrolyzing cell 2 through line 3.
- a vent gas stream 4 is also withdrawn from the electrolyzing cell 2.
- the vent gas stream 4 comprises O 2 , CO 2 , N 2 , F 2 , HF, NaAlF 4 , CF 4 , C 2 F 6 , and particulates.
- the vent gas stream 4 is optionally passed to a filter 5 to remove the particulates therein.
- a filtered vent gas 6 is optionally withdrawn from filter 5 and passed to a dry scrubbing zone 7.
- the filtered vent gas 6 is contacted with alumina introduced through line 8 at conditions effective to remove inorganic fluorides such as F 2 and HF therefrom.
- F 2 and HF inorganic fluorides
- the alumina reacts with F 2 and HF in the filtered vent gas 6 to form aluminum trifluoride according to the following equations: Al 2 O 3 + F 2 AlF 3 + O 2 Al 2 O 3 + HF AlF 3 + H 2 O
- a stream 9 comprising the aluminum trifluoride is then withdrawn from the dry scrubbing zone 7 and recycled to stream 1.
- the dry scrubbing zone 7 also yields a purified vent gas stream 10 containing CF 4 , C 2 F 6 , O 2 , CO 2 , and N 2 .
- Stream 10 is passed to an additional filter 11, if necessary, to remove any remaining particulates therein.
- the purified vent gas stream 10 is next passed to a membrane separation system 12 such as the one described above and illustrated in Figure 3 where a retentate stream 14 and a permeate stream 13 are produced.
- the permeate stream 13 comprises mostly of O 2 , CO 2 , and N 2
- the retentate stream 14 comprises mostly of CF 4 and C 2 F 6 .
- the retentate stream 14 comprising CF 4 and C 2 F 6 may be further purified on or off-site to produce a CF 4 /C 2 F 6 stream suitable for use in the semiconductor industry.
- a gas stream comprising CF 4 , C 2 F 6 , and N 2 was contacted with a polyimide, asymmetric composite hollow fiber membrane at various temperatures to measure the relative permeabilities of CF 4 , C 2 F 6 , and N 2 .
- the gas stream had a constant flowrate of 170 mL/min.
- the pressure of the feed gas was kept constant at 3 bar.
- the permeabilities of each of these components are graphically shown in Figure 2. As seen from Figure 2, the selectivities of CF 4 /N 2 and C 2 F 6 /N 2 are on the order of 300.
- Example 2 The procedure of Example 1 was repeated using the feed concentration and pressure listed in Table 2 below. The simulated results are also listed in Table 2.
- the flowrate of the vent gas is about 3 Nm 3 /h.
- the same procedure of Example 1 was followed using such a stream.
- the feed concentration and pressure as well as the simulated results of such a stream are reported in Table 3 below.
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- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Metallurgy (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- General Chemical & Material Sciences (AREA)
- Electrochemistry (AREA)
- Materials Engineering (AREA)
- Analytical Chemistry (AREA)
- Organic Chemistry (AREA)
- Separation Using Semi-Permeable Membranes (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Treating Waste Gases (AREA)
- Compounds Of Alkaline-Earth Elements, Aluminum Or Rare-Earth Metals (AREA)
- Electrolytic Production Of Non-Metals, Compounds, Apparatuses Therefor (AREA)
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US08/772,469 US5814127A (en) | 1996-12-23 | 1996-12-23 | Process for recovering CF4 and C2 F6 from a gas |
US772469 | 1996-12-23 | ||
PCT/US1997/022306 WO1998028062A1 (en) | 1996-12-23 | 1997-12-16 | Process for recovering cf4 and c2f6 from a gas |
Publications (2)
Publication Number | Publication Date |
---|---|
EP0951337A1 EP0951337A1 (en) | 1999-10-27 |
EP0951337B1 true EP0951337B1 (en) | 2003-02-05 |
Family
ID=25095170
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP97952294A Expired - Lifetime EP0951337B1 (en) | 1996-12-23 | 1997-12-16 | Process for recovering cf 4? and c 2?f 6? from a gas |
Country Status (13)
Country | Link |
---|---|
US (2) | US5814127A (xx) |
EP (1) | EP0951337B1 (xx) |
JP (1) | JP3274474B2 (xx) |
CN (1) | CN1244813A (xx) |
AT (1) | ATE232132T1 (xx) |
AU (1) | AU715057B2 (xx) |
BR (1) | BR9713633A (xx) |
CA (1) | CA2275907C (xx) |
DE (1) | DE69718933T2 (xx) |
ES (1) | ES2192276T3 (xx) |
NO (1) | NO321288B1 (xx) |
PL (1) | PL334243A1 (xx) |
WO (1) | WO1998028062A1 (xx) |
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US6187077B1 (en) * | 1998-04-17 | 2001-02-13 | American Air Liquide Inc. | Separation of CF4 and C2F6 from a perfluorocompound mixture |
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-
1996
- 1996-12-23 US US08/772,469 patent/US5814127A/en not_active Expired - Fee Related
-
1997
- 1997-12-16 AU AU55937/98A patent/AU715057B2/en not_active Ceased
- 1997-12-16 EP EP97952294A patent/EP0951337B1/en not_active Expired - Lifetime
- 1997-12-16 WO PCT/US1997/022306 patent/WO1998028062A1/en not_active Application Discontinuation
- 1997-12-16 BR BR9713633-6A patent/BR9713633A/pt not_active Application Discontinuation
- 1997-12-16 CN CN97181383A patent/CN1244813A/zh active Pending
- 1997-12-16 JP JP52878598A patent/JP3274474B2/ja not_active Expired - Fee Related
- 1997-12-16 AT AT97952294T patent/ATE232132T1/de not_active IP Right Cessation
- 1997-12-16 ES ES97952294T patent/ES2192276T3/es not_active Expired - Lifetime
- 1997-12-16 CA CA002275907A patent/CA2275907C/en not_active Expired - Fee Related
- 1997-12-16 DE DE69718933T patent/DE69718933T2/de not_active Expired - Fee Related
- 1997-12-16 PL PL97334243A patent/PL334243A1/xx unknown
-
1998
- 1998-05-01 US US09/071,200 patent/US5968334A/en not_active Expired - Fee Related
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1999
- 1999-06-18 NO NO19992990A patent/NO321288B1/no not_active IP Right Cessation
Also Published As
Publication number | Publication date |
---|---|
AU5593798A (en) | 1998-07-17 |
JP2000509653A (ja) | 2000-08-02 |
DE69718933T2 (de) | 2003-12-24 |
NO992990L (no) | 1999-08-20 |
CN1244813A (zh) | 2000-02-16 |
CA2275907C (en) | 2005-11-15 |
EP0951337A1 (en) | 1999-10-27 |
NO321288B1 (no) | 2006-04-18 |
DE69718933D1 (de) | 2003-03-13 |
AU715057B2 (en) | 2000-01-13 |
NO992990D0 (no) | 1999-06-18 |
US5968334A (en) | 1999-10-19 |
US5814127A (en) | 1998-09-29 |
CA2275907A1 (en) | 1998-07-02 |
WO1998028062A1 (en) | 1998-07-02 |
ES2192276T3 (es) | 2003-10-01 |
JP3274474B2 (ja) | 2002-04-15 |
PL334243A1 (en) | 2000-02-14 |
BR9713633A (pt) | 2000-04-11 |
ATE232132T1 (de) | 2003-02-15 |
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